ライフサイエンスコーパス: poplar

1 ncentrations (e.g., 1 mg/L of 5 nm AgNPs for poplar).

2 centrations (e.g., 1 mg/L of 25 nm AgNPs for poplar).

3 er the split between legumes and Salicaceae (poplar).

4 and 78 mole % for a high-syringyl transgenic poplar).

5 tes and its xylem-specific introduction into poplar.

6 13.8 times higher than with untreated yellow poplar.

7 variation of lignocellulosic traits in black poplar.

8 ion factors during secondary woody growth in poplar.

9 olved in the regulation of wood formation in poplar.

10 reliable marker in woody angiosperms such as poplar.

11 gulatory mechanism in response to drought in poplar.

12 from cinnamoyl CoA reductase (CCR)-deficient poplar.

13 occurred after the split of Arabidopsis and poplar.

14 nscript is rare during the juvenile phase of poplar.

15 ontrols first-time and seasonal flowering in poplar.

16 n, ending the juvenile phase, are unknown in poplar.

17 the development of woody characteristics in poplar.

18 e over-expressed the F5H gene in tobacco and poplar.

19 ry network for proanthocyanidin synthesis in poplar.

20 ge-based functional genomics and breeding of poplar.

21 amic nitrogen foraging in biofuel crops like poplar.

22 -1), was enantioselectively removed in whole poplar.

23 sive loading of Suc through plasmodesmata in poplar.

24 equally transported and metabolized in whole poplars.

25 ey were detected in various tissues of whole poplars.

26 onship to the formation of OH-PCB3s in whole poplars.

27 PCB3 metabolites into PCB3 sulfates in whole poplars.

28 transformation products (OH-PCB3s) in whole poplars.

29 arp decreases of OH-PCB3s formation in whole poplars.

30 iosynthesis (xylogenesis) in Arabidopsis and poplars.

31 an opposite response as compared to that in poplars.

32 ucts could be detected in the CAD1-deficient poplars.

33 mistletoe growing on trees such as apples or poplars.

34 le to the toxic effects of Ag(+) (1 mg/L for poplar, 0.05 mg/L for Arabidopsis), but AgNPs also showe

35 ntrations (e.g., 100 mg/L of 25 nm AgNPs for poplar, 1 mg/L of 5 nm AgNPs for Arabidopsis) and this s

36 ed test beds were planted with 12 transgenic poplars, 12 wild type (WT) poplars, or left unplanted, a

37 el plant systems has now been transferred to poplar, a species with field applicability.

38 than in the stem or flower tissues), whereas poplars accumulated silver at similar concentrations in

39 and PAs are effective antifungal defenses in poplar against foliar rust infection.

40 For Medicago, poplar and Arabidopsis, but not in rice, alternative spl

41 g Arabidopsis, Brachypodium, maize, sorghum, poplar and grape in addition to several species of rice.

42 The use of poplar and hickory led to a decrease in the PAH contents

43 omparisons of the DAM gene promoters between poplar and leafy spurge have identified several conserve

44 alyzed was also slightly higher than that in poplar and papaya.

45 ield and in a wider range of plants, such as poplar and perennial grasses.

46 is part of the flower initiation pathway in poplar and plays an additional role in regulating season

47 Furthermore, FBH homologs in poplar and rice induced CO expression in Arabidopsis.

48 ees among rice, Arabidopsis thaliana, maize, poplar and several animal species (for reference purpose

49 Both poplars and Arabidopsis accumulated silver, but silver d

50 truncatula (Medicago), Populus trichocarpa (poplar) and Arabidopsis thaliana (Arabidopsis), and the

51 del tree' genus Populus: Populus alba (white poplar) and Populus tremula (European aspen).

52 anic inputs; three perennial crops (alfalfa, poplar, and conifers); and four unmanaged ecosystems of

53 ng the sequenced rosids Arabidopsis, papaya, poplar, and grape.

54 cterial isolates from roots of Brassicaceae, poplar, and maize.

55 sorbed, taken up, and translocated in whole poplars, and they were detected in various tissues of wh

56 is incorporated into lignin in angiosperms (poplar, Arabidopsis, tobacco), has been structurally ide

57 These studies also highlight poplar as an alternative sequenced model for spatiotempo

58 erence in regulation between Arabidopsis and poplars as differential regulation.

59 ibed here is from studies of fruit trees and poplar, as these species have been the primary subjects

60 which metabolized PCB3 to OH-PCB3s in whole poplars because suicide CYP inhibitors ABT and ODYA both

61 * We conclude that poplar branches comprise modules that are relatively ind

62 These results indicate that although poplar BSP is encoded by a multigene family, transcripti

63 roteins of poplar share some similarities to poplar BSP, the observed developmental expression patter

64 Poplar BSPs are encoded by a multigene family and one me

65 y important for the lignification process in poplar but is also a promising target for the developmen

66 examined patterns of gene expression in the poplar C-repeat binding factor (CBF) gene family.

67 ectivity of chiral OH-PCBs and suggests that poplars can enantioselectively biotransform at least one

68 r formation, we sequenced the genomes of the poplar canker pathogen, Mycosphaerella populorum, and th

69 Some Poplar CBF homologs exhibited patterns consistent with h

70 Transient promoter activation assays in poplar cell culture demonstrated that MYB182 can disrupt

71 It is concluded that in poplar cells: (a) exogenously supplied Orn enters the ce

72 demonstrated that the ozone-sensitive hybrid poplar clone NE-388 displays an attenuated level of ozon

73 CaMV 35S promoter was expressed in a hybrid poplar clone, Populus x euramericana ('Ogy').

74 Trees in the genus Populus (poplar) contain phenolic secondary metabolites including

75 from the industrially contaminated East Fork Poplar Creek, Tennessee (EFPC) were measured during 2014

76 on was revealed between a pair of duplicated poplar Dof genes, which have identical motif structure a

77 Poplar DQD/SDHs have distinct expression profiles sugges

78 ined nearly racemic in most tissues of whole poplars during 10 day exposure, suggesting the enantiome

79 A survey of poplar EST sequences showed that MADS-box genes were exp

80 ed through simulation studies that mimic the poplar example used.

81 0,000 BAC clones for mouse, rat, bovine, and poplar fingerprint mapping projects.

82 Here, we report that poplar FLOWERING LOCUS T2 (FT2), a relative of the Arabi

83 However, the enantioselectivity of poplar for 5-OH-PCB91 and 5-OH-PCB95 proved to be quite

84 e impact that the large-scale cultivation of poplar for use as a biofuel feedstock will have on air q

85 to evaluate the effectiveness of transgenic poplars for phytoremediation.

86 volving and interactive genes that determine poplar-fungus interactions are identified.

87 ddition, RNA interference suppression of two poplar GA 2-oxidases predominantly expressed in roots al

88 Poplar gene and enhancer traps provide a new resource th

89 The poplar genome encodes five DQD/SDH-like genes (Poptr1 to

90 e studies, and addition of SSR loci from the poplar genome project provided coarse alignment with the

91 Investigation of the poplar genome revealed 105 putative functional MADS-box

92 s plant biologists to directly reference the poplar genome sequence and identify novel genes of inter

93 e (GUS) reporter gene were inserted into the poplar genome via Agrobacterium tumefaciens transformati

94 70% more than Arabidopsis and similar to the poplar genome which, like soybean, is an ancient polyplo

95 rated the absence of additional genes in the poplar genome with significant PTAG1/2 homology.

96 gus grandifolia 454 ESTs and unigenes to the poplar genome.

97 ist at least two MIKC* MADS-box genes in the poplar genome.

98 each of these genes has a counterpart in the poplar genomic database along with additional members of

99 were highly responsive to the CCR-deficient poplar genotype with remarkably different metabolic capa

100 leaf growth, and overall carbon (C) gain of poplar genotypes emitting (IE) and nonemitting (NE) isop

101 Poplar genotypes with constitutively higher levels of ca

102 In poplar (genus Populus), MYB134 is known to regulate proa

103 relatives, PBS3 syntelogs are identified in poplar, grape, columbine, maize and rice suggesting desc

104 Endophytes isolated from native poplar growing in nutrient-poor conditions were selected

105 Poplar has 192 annotated R2R3 MYB genes, of which only t

106 However, poplar has 64 type II MADS-box genes, implying a higher

107 volved in the hydroxylation of PCB3 in whole poplars have not been identified.

108 he 51 smoking experiments wood chips of oak, poplar, hickory, spruce, fir, alder, beech, and beech wi

109 report the characterization of PtrMYB152, a poplar homolog of the Arabidopsis R2R3 MYB transcription

110 We examined nucleotide diversity of 27 poplar homologs of the flowering-time network-a group of

111 ombinant PcISPS (isoprene synthase from gray poplar hybrid Populusxcanescens) has been determined at

112 r of sylleptic branches on the main stems of poplar hybrids by a Poisson distribution, the new model

113 erimental data for 29 commercially available poplar hybrids to assess the impact that the large-scale

114 ed kinetic properties similar to AtIAMT1 and poplar IAMT (PtIAMT1).

115 itive and dominant, on the dynamic growth of poplar in diameter and height.

116 the hydroxylation reaction of PCB3 in whole poplars in this work.

117 and characterizing dosage-based variation in poplar, including the contribution of dosage to quantita

118 Overexpression of PdRanBP in poplar increased the number of sylleptic branches and th

119 eminated intraspecific F1 seeds of Euphrates Poplar individually in a tube to obtain a total of 370 s

120 When juvenile poplar is transformed with FT2 and transcript levels are

121 Populus trichocarpa (poplar) is distinguished from its herbaceous counterpart

122 The inferred yellow-poplar laccase gene products were highly related to one

123 thern blot analysis revealed that the yellow-poplar laccase genes are differentially expressed in xyl

124 TP-binding cassette transporter CpMRP of the poplar leaf beetle, Chrysomela populi as the first candi

125 phaerella populorum, and the closely related poplar leaf pathogen, M. populicola.

126 esized catechin and PAs in the rust-infected poplar leaves accumulated significantly at the site of f

127 ed after feeding sulfate and ABA to detached poplar leaves and epidermal peels of Arabidopsis (Arabid

128 urray's rule, and that the phloem network in poplar leaves can generate the pressure gradient envisio

129 oasted ore waste, calcine (roasted ore), and poplar leaves collected at a closed Hg mine (New Idria,

130 The poplar leaves exhibited negative MDF (-3.18 to -1.22 per

131 ork was validated by a pathological study of poplar leaves infected by fungal Marssonina brunnea in w

132 sion values were verified against GBW 07604 (Poplar leaves) certified reference material and by the r

133 raviolet light stress has been documented in poplar leaves, and a regulator of this process, the R2R3

134 of MEP pathway intermediates in mature gray poplar leaves, and its production required severalfold h

135 ts of both MYB115- and MYB134-overexpressing poplar led to the discovery of enhanced flavonoid B-ring

136 The poplar lines developed here also outperformed controls u

137 case isoenzymes from xylem tissues of yellow-poplar (Ltlacc2.1-4) were identified and sequenced.

138 Like other gene families, poplar MADS-box gene family has expanded through tandem

139 Poplar MADS-box genes were distributed on all linkage gr

140 : Lauraceae), Liriodendron tulipifera (tulip poplar: Magnoliaceae), and Saruma henryi (Aristolochiace

141 and extensive root systems, these transgenic poplars may provide the means to effectively remediate s

142 observations and allowed us to identify the poplar members most responsive to heat stress.

143 beneficial function of isoprene emission in poplar might be of minor importance to mitigate predicte

144 In poplars, miR398 was first induced upon 3-4 h of ABA or s

145 second PVX strain and the distantly related poplar mosaic virus (PopMV).

146 s investigated by transforming either hybrid poplar or tobacco with a chimeric gene consisting of the

147 ith 12 transgenic poplars, 12 wild type (WT) poplars, or left unplanted, and dosed with equivalent co

148 s of transcript levels for the 10 members in poplar organs indicate that most genes are constitutivel

149 well as with earlier evidence showing that a poplar ortholog is reduced by a glutaredoxin rather than

150 ingle-nucleotide polymorphisms (SNPs) in the poplar ortholog of the class III homeodomain-leucine zip

151 interference (RNAi)-mediated suppression of poplar orthologs of CEN, and the related gene MOTHER OF

152 we report the functional characterization of poplar orthologs of MYB46 and MYB83 that are known to be

153 Transgenic poplar overexpressing MYB115 showed a high-proanthocyani

154 racterized by ectopic expression in a hybrid poplar (P. davidiana Dode x P. bolleana Lauche).

155 ons and yields of five OH-PCB3s in different poplar parts via the inhibition of CYPs.

156 ' plants were inoculated with conidia of the poplar pathogenic fungus Septoria musiva, which produces

157 two proteins based on crystal structures of poplar PC and turnip cyt f at pH 7 and a variety of ioni

158 lower initiation that is integrated with the poplar perennial growth habit.

159 We measured gene flow from hybrid poplar plantations using morphological and genetic marke

160 re strongly dependent on the location of the poplar plantations, due to the prevailing meteorology, t

161 In this study, poplar plants (Populus x canescens) were exposed to wate

162 er by endogenous sHSPs in both heat-stressed poplar plants and field-grown adult trees.

163 sion by the antisense approach in transgenic poplar plants caused a significant decrease in total lig

164 Results showed poplar plants could metabolize PCB3 into PCB3 sulfates d

165 The transgenic poplar plants exhibited increased removal rates of these

166 nalysis of MYB115- and MYB134-overexpressing poplar plants identified a set of common up-regulated ge

167 ated metabolites of PCB3 (OH-PCB3s) in whole poplar plants in our previous work.

168 on of MYB182 in hairy root culture and whole poplar plants led to reduced PA and anthocyanin levels a

169 esis were further demonstrated in transgenic poplar plants showing an ectopic deposition of secondary

170 We show that transgenic poplar plants with dominant repression of PtrWNDs functi

171 this coordination group were investigated in poplar plastocyanin (Pcy) by mutation of a conserved ele

172 cucumber stellacyanin, P. aeruginosa azurin, poplar plastocyanin, C. cinereus laccase, T. ferrooxidan

173 ntial of P. aeruginosa azurin as compared to poplar plastocyanin, whereas the reverse is true for C.

174 cots, Arabidopsis (Arabidopsis thaliana) and poplar (Populus alba x grandidentata), and a series of a

175 Using balsam poplar (Populus balsamifera) as a case study, we demonst

176 idopsis thaliana. AC079673 and AB016886) and poplar (Populus balsamifera, AI166543).

177 Poplar (Populus deltoides x nigra, DN34) was used to inv

178 isoprene emission in oak (Quercus robur) and poplar (Populus deltoides) leaves in order to understand

179 Many woody perennials, such as poplar (Populus deltoides), are not able to form flower

180 c (Medicago truncatula, dicot, Leguminosae), poplar (Populus deltoides, dicot, Salicaceae), and switc

181 nducted a mapping experiment using Euphrates poplar (Populus euphratica), a so-called hero tree able

182 C4H2 shows highest similarity to a poplar (Populus kitakamiensis) sequence, but also shows

183 ransgenic (NT) and a transgenic cell line of poplar (Populus nigra x maximowiczii) expressing a mouse

184 non-transgenic (NT) and transgenic cells of poplar (Populus nigra x maximowiczii) expressing a mouse

185 Black poplar (Populus nigra) is a potential feedstock for cell

186 antifungal activity of flavan-3-ols in black poplar (Populus nigra), which include both monomers, suc

187 gatum), corn stover, sugar cane bagasse, and poplar (Populus sp.).

188 Elite poplar (Populus spp) varieties are created through inter

189 BER) is one of the most abundant proteins in poplar (Populus spp) xylem, but its biological role has

190 ealed that IAMTs from Arabidopsis, rice, and poplar (Populus spp.) form a monophyletic group.

191 iochemical properties of some representative poplar (Populus spp.) isoforms were investigated.

192 Isoprene emissions from poplar (Populus spp.) plantations can influence atmosphe

193 Specifically, in poplar (Populus spp.), the formation of xylem embolisms

194 ism, signaling, and response are affected in poplar (Populus spp.)-Laccaria bicolor ECM roots.

195 e and reproductive growth in woody perennial poplar (Populus spp.).

196 ae, Solanaceae, additional cereal crops, and poplar (Populus spp.).

197 nin content and composition were modified in poplar (Populus tremula x Populus alba) by specifically

198 sequently characterized an activation-tagged poplar (Populus tremula x Populus alba) mutant with enha

199 We have developed transgenic poplar (Populus tremula x Populus alba) plants with grea

200 is essential in lignin biosynthesis in woody poplar (Populus tremula x Populus alba) plants.

201 e show that down-regulation of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up t

202 previously poorly characterized response of poplar (Populus tremula x Populus alba) roots to low nit

203 provide experimental evidence that, in gray poplar (Populus tremula x Populus alba), Suc enters the

204 Using hybrid poplar (Populus tremula x Populus alba), we applied this

205 in 2-year-old high-density stands of hybrid poplar (Populus tremula x Populus alba).

206 le increase in the thermotolerance of hybrid poplar (Populus tremulaxPopulus alba) through overexpres

207 ciation studies of approximately 400 natural poplar (Populus trichocarpa) accessions phenotyped for 6

208 enomes - Arabidopsis (Arabidopsis thaliana), poplar (Populus trichocarpa) and rice (Oryza sativa).

209 maize, rice (Oryza sativa), Arabidopsis, and poplar (Populus trichocarpa) revealed a core binding sit

210 Solanum tuberosum), Medicago truncatula, and poplar (Populus trichocarpa) revealed conserved ratios o

211 ding with one finger) protein sequences from poplar (Populus trichocarpa) Torr.

212 ovide direct evidence demonstrating that the poplar (Populus trichocarpa) wood-associated NAC domain

213 report on a screen of natural accessions of poplar (Populus trichocarpa), revealing that the leaf cu

214 which over 40% had up-regulated orthologs in poplar (Populus trichocarpa), rice (Oryza sativa), or Ch

215 es of Arabidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa), two near-complete rosid ge

216 induced aldoxime formation in western balsam poplar (Populus trichocarpa).

217 erved in spruce, grape (Vitis vinifera), and poplar (Populus trichocarpa).

218 cies, Arabidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa).

219 dventitious root formation in the model tree poplar (Populus trichocarpa).

220 eferentially expressed in developing wood of poplar (Populus trichocarpa).

221 me of IE and non-isoprene-emitting (NE) gray poplar (Populus x canescens) after acute ozone fumigatio

222 Knockdown lines of CYP79D6/7 in gray poplar (Populus x canescens) exhibited a decreased emiss

223 Rays from wood samples of poplar (Populus x canescens) were enriched by laser micr

224 -emitting (IE) and nonisoprene-emitting (NE) poplar (Populus x canescens).

225 Here, we pair work in poplar (Populus) describing one of the smallest sex-dete

226 is a major goal for bioenergy crops, such as poplar (Populus), which will be grown on marginal lands

227 In this study, poplars (Populus deltoides x nigra) and Arabidopsis thal

228 Poplars (Populus deltoides x nigra, DN34) were exposed t

229 Poplars (Populus deltoides x nigra, DN34), a model plant

230 Field study of transgenic poplars (Populus spp.) for over 6 years showed that down

231 largely based upon our long-term studies of poplars (Populus spp.).

232 Poplars (Populus tremula x Populus alba) down-regulated

233 te profiles and physiological performance in poplars (Populus x canescens) with either wild-type or R

234 gues describes the development of transgenic poplars (Populus) overexpressing a mammalian cytochrome

235 In poplars (Populus), bspA encodes a 32-kD bark storage pro

236 rabidopsis thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], and grape [Vitis vinifera]

237 idate genes for adaptive phenology in balsam poplar, Populus balsamifera, a widespread forest tree wh

238 nd transgenic isoprene-nonemitting (NE) gray poplar (Populusxcanescens).

239 her SUT4-RNAi directly or indirectly altered poplar predisposition and/or response to changes in soil

240 Consistently, expression of both of the poplar Proline Dehydrogenase orthologs and two of the Fl

241 n showed that the phenotype is caused by the poplar PtabZIP1-like (PtabZIP1L) gene with highest homol

242 rly post-pollination response in this hybrid poplar reproduction.

243 To determine their role in poplar response to water stress, transgenic Populus trem

244 These images of the poplar rhizosphere showed evidence for symbiotic sharing

245 lant species including Arabidopsis, tobacco, poplar, rice, Eastern cottonwood, peanut, salt marsh gra

246 trate that PtAIL1 is a positive regulator of poplar rooting that acts early in the development of adv

247 ate, and 4'-PCB3 sulfate, were identified in poplar roots and their concentrations increased in the r

248 Transgenic poplar samples that overexpressed PtAIL1 were able to gr

249 le tissues of unbranched and branched hybrid poplar saplings (Populus nigra x P. deltoides).

250 * In poplar saplings with multiple lateral branches, we obser

251 The use of the rapidly growing poplar seems to be a reasonable approach for reducing th

252 re within and between rust species on Linum, poplar, Senecio, wheat, and several grass species.

253 Together the results suggest a role for poplar SEP-class genes in reproductive viability.

254 Although seed storage proteins of poplar share some similarities to poplar BSP, the observ

255 upon root uptake, and their translocation to poplar shoots (negligible for PAA-EG-QDs and 0.7 ng Cd/m

256 ynthase gene structure was analysed in three poplar species.

257 In poplar, specifically, the addition of these conjugates d

258 Incubation of steam-pretreated poplar (SPP) with sLac enhanced the release of acid-prec

259 gricultural site planted with a high-density poplar stand.

260 In poplar stems, CCoAOMT was found to be expressed in all l

261 in planta produced Xyl10B was detected with poplar, sweetgum and birchwood xylan substrates followin

262 In transformed poplar, the bspA 2.8 kb promoter conferred both short-da

263 concentration range, silver accumulation in poplar tissues increased with exposure concentration and

264 tly enantioselectively biotransformed inside poplar tissues, in contrast to nearly racemic mixtures o

265 In this study, poplars transformed with a chimeric gene consisting of t

266 When a single leaf on a young poplar tree is mechanically wounded, wound-induced (win)

267 grading endophytic bacteria and fast-growing poplar tree systems offers a readily deployable, cost-ef

268 In this study, poplar trees (Populus deltoides x nigra) were exposed hy

269 t effects of field-grown, CCR-down-regulated poplar trees (Populus tremula x Populus alba) on the bac

270 P influences the apical and radial growth of poplar trees and that PdRanBP may regulate cell division

271 e SNPs are studied, and the phenotypes of 64 poplar trees are recorded.

272 We report a gene discovery system for poplar trees based on gene and enhancer traps.

273 Transgenic poplar trees carrying the C4H-F5H transgene also display

274 his work, metabolite profiling of transgenic poplar trees downregulated in PCBER revealed both the in

275 The inoculated poplar trees exhibited increased growth and reduced TCE

276 izosphere microbiome of CCR-deficient and WT poplar trees featured highly overlapping bacterial commu

277 Poplar trees that were inoculated with the biotrophic ru

278 We have engineered poplar trees to introduce ester linkages into the lignin

279 endophyte, Enterobacter sp. strain PDN3, of poplar trees, that rapidly metabolizes TCE, releasing ch

280 iosynthetic program during wood formation in poplar trees.

281 into the steps underlying the seasonality of poplar trees.

282 diameter compared to mock-inoculated control poplar trees.

283 acid) that are up-regulated in CCR-deficient poplar trees.

284 reference species: Arabidopsis thaliana and Poplar trichocarpa.

285 pseudogenes were found, suggesting that the poplar type I MADS-box genes have experienced a lower ra

286 e genetic control of bud phenology in hybrid poplar was studied by mapping quantitative trait loci (Q

287 tivation tagging in the prime bioenergy crop poplar, we have identified a mutant that overcomes the b

288 phenolic substances in sausages smoked with poplar were higher, or only slightly lower, when compare

289 namic diameter and height growth patterns of poplar were systematically analyzed.

290 nse-related symptoms in leaves of transgenic poplar when the plants were abruptly exposed to excessiv

291 However, the function of RanBP in poplar, which has very typical secondary growth, remains

292 issection, and transcripts were monitored by poplar whole-genome microarrays.

293 Pretreatment of yellow poplar with peracetic acid (300 mM, 2.3 wt%) and dilute

294 Transgenic poplars with RNAi-suppressed PtaSUT4 exhibited increased

295 um is fully activated following induction by poplar wood and leaves.

296 estigated the fate of trace elements (TE) in poplar wood on the conversion of biomass to heat in a 0.

297 ical properties and dimensional stability of poplar wood were examined.

298 ivate the promoter activities of a number of poplar wood-associated transcription factors and wood bi

299 were up-regulated in M. populorum growing on poplar wood-chip medium compared with M. populicola.

300 to infect, colonize, and cause mortality on poplar woody stems.